ORCID Profile
0000-0002-7046-3057
Current Organisation
University of Helsinki
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Publisher: Copernicus GmbH
Date: 08-10-2021
DOI: 10.5194/ACP-2021-744
Abstract: Abstract. The formation of ice particles in Earth’s atmosphere strongly influences the dynamics and optical properties of clouds and their impacts on the climate system. Ice formation in clouds is often triggered heterogeneously by ice nucleating particles (INPs) that represent a very low number of particles in the atmosphere. To date, many sources of INPs, such as mineral and soil dust, have been investigated and identified in the lower latitudes. Although less is known about the sources of ice nucleation at higher latitudes, efforts have been made to identify the sources of INPs in the Arctic and boreal environments. In this study, we investigate the INP emission potential from high latitude boreal forests. We introduce the HyICE-2018 measurement c aign conducted in the boreal forest of Hyytiälä, Finland between February and June 2018. The c aign utilized the infrastructure of the SMEAR II research station with additional instrumentation for measuring INPs to quantify the concentrations and sources of INPs in the boreal environment. In this contribution, we describe the measurement infrastructure and operating procedures during HyICE-2018 and we report results from specific time periods where INP instruments were run in parallel for inter-comparison purposes. Our results show that the suite of instruments deployed during HyICE-2018 reports consistent results and therefore lays the foundation for forthcoming results to be considered holistically. In addition, we compare the INP concentration we measured to INP parameterizations, and we show a very good agreement with the Tobo et al. (2013) parameterization developed from measurements conducted in a ponderosa pine forest ecosystem in Colorado, USA.
Publisher: Copernicus GmbH
Date: 08-05-2023
Publisher: Copernicus GmbH
Date: 15-05-2023
DOI: 10.5194/EGUSPHERE-EGU23-8058
Abstract: Understanding ocean-cloud interactions and their effect on climate requires that atmospheric new particle formation is characterized. Yet, the process of particle formation from marine biogenic gaz-phase emissions has not been evidenced in the open ocean lower atmosphere, partly due to the naturally low concentrations of these particles in remote oceanic places. Here we show, using new ship-borne air-sea interface enclosures, that new particles are formed in relation to marine micro-biology present in the seawater. The chemical analysis of newly formed clusters with API-ToF-MS shows unexpected results, implicating nucleating coumpounds and pathways that are usually not taken into account in nucleation processes.
Publisher: Copernicus GmbH
Date: 04-03-2021
DOI: 10.5194/EGUSPHERE-EGU21-8110
Abstract: & & Even though oceans cover over 70% of the Earth& #8217 s surface, the ways in which oceans interact with climate are not fully known. Marine micro-organisms such as phytoplankton can play an important role in regulating climate by releasing different chemical species into air. In air these chemical species can react and form new aerosol particles. If grown to large enough sizes, aerosols can influence climate by acting as cloud condensation nuclei which influence the formation and properties of clouds. Even though a connection of marine biology and climate through aerosol formation was first proposed already over 30 years ago, the processes related to this connection are still uncertain.& & & & To unravel how seawater properties affect aerosol formation and to identify which chemical species are responsible for aerosol formation, we built two Air-Sea-Interaction Tanks (ASIT) that isolate 1000 l of seawater and 1000 l of air directly above the water. The used seawater was collected from different locations during a ship c aign on board the R/V Tangaroa in the South West Pacific Ocean, close to Chatham Rise, east of New Zealand. Seawater from one location was kept in the tanks for 2-3 days and then changed. By using seawater collected from different locations, we could obtain water with different biological populations. To monitor the seawater, we took daily s les to determine its chemical and biological properties.& & & & The air in the tanks was continuously flushed with particle filtered air. This way the air had on average 40 min to interact with the seawater surface before being s led. Our air s ling was continuous and consisted of aerosol and air chemistry measurements. The instrumentation included measurements of aerosol number concentration from 1 to 500 nm and& chemical species ranging from ozone and sulphur dioxide to volatile organic compounds and chemical composition of molecular clusters.& & & & Joining the seawater and atmospheric data together can give us an idea of what chemical species are emitted from the water into the atmosphere and whether these species can form new aerosol particles. Our preliminary results show a small number of particles in the freshly nucleated size range of 1-3 nm in the ASIT headspaces, indicating that new aerosol particles can form in the ASIT headspaces. In this presentation, we will also explore which chemical species could be responsible for aerosol formation and which plankton groups could be related to the emissions of these species. Combining these results with ambient data and modelling work can shed light on how important new particle formation from marine sources is for climate.& & & & Acknowledgements: Sea2Cloud project is funded by European Research Council (ERC) under the European Union& #8217 s Horizon 2020 research and innovation programme (Grant agreement No. 771369).& &
Publisher: Copernicus GmbH
Date: 19-04-2022
Abstract: Abstract. The formation of ice particles in Earth's atmosphere strongly influences the dynamics and optical properties of clouds and their impacts on the climate system. Ice formation in clouds is often triggered heterogeneously by ice-nucleating particles (INPs) that represent a very low number of particles in the atmosphere. To date, many sources of INPs, such as mineral and soil dust, have been investigated and identified in the low and mid latitudes. Although less is known about the sources of ice nucleation at high latitudes, efforts have been made to identify the sources of INPs in the Arctic and boreal environments. In this study, we investigate the INP emission potential from high-latitude boreal forests in the mixed-phase cloud regime. We introduce the HyICE-2018 measurement c aign conducted in the boreal forest of Hyytiälä, Finland, between February and June 2018. The c aign utilized the infrastructure of the Station for Measuring Ecosystem-Atmosphere Relations (SMEAR) II, with additional INP instruments, including the Portable Ice Nucleation Chamber I and II (PINC and PINCii), the SPectrometer for Ice Nuclei (SPIN), the Portable Ice Nucleation Experiment (PINE), the Ice Nucleation SpEctrometer of the Karlsruhe Institute of Technology (INSEKT) and the Microlitre Nucleation by Immersed Particle Instrument (µL-NIPI), used to quantify the INP concentrations and sources in the boreal environment. In this contribution, we describe the measurement infrastructure and operating procedures during HyICE-2018, and we report results from specific time periods where INP instruments were run in parallel for inter-comparison purposes. Our results show that the suite of instruments deployed during HyICE-2018 reports consistent results and therefore lays the foundation for forthcoming results to be considered holistically. In addition, we compare measured INP concentrations to INP parameterizations, and we observe good agreement with the Tobo et al. (2013) parameterization developed from measurements conducted in a ponderosa pine forest ecosystem in Colorado, USA.
Publisher: Springer International Publishing
Date: 2021
Publisher: Copernicus GmbH
Date: 08-05-2023
DOI: 10.5194/EGUSPHERE-2023-516
Abstract: Abstract. Air-sea fluxes of dimethyl sulphide (DMS) and methanethiol (MeSH) from surface seawater in the remote Southern Pacific Ocean were measured in three Air-Sea Interface Tank (ASIT) experiments during the Sea2Cloud voyage in March 2020. The measured fluxes of 0.78 ± 0.44 ng m-2 s-1 and 0.05 ± 0.03 ng m-2 s-1 for DMS and MeSH, respectively, varied between experiments reflecting the different water mass types investigated, with lowest fluxes with subtropical water and highest with biologically-active water with sub-Tropical water and highest from the sub-Tropical Front. Measured DMS fluxes were consistent with calculated fluxes from a two-layer model using DMS concentration in the ASIT seawater. The experiments also determined the influence of elevated ozone, with one ASIT headspace amended with 10 ppbv ozone while the other provided an unamended control. Elevated ozone resulted in a decrease in DMS flux, corresponding to decreased conversion of dimethylsulfoniopropionate (DMSP) to DMS in the seawater. The MeSH:DMS flux range was 11–18 % across experiments, in line with previous observations, indicating that MeSH represents a significant contribution to the atmospheric sulfur budget. Using the ASIT results in combination with ambient seawater concentrations during Sea2Cloud, significant linear correlations were identified for both DMS and MeSH fluxes with nanophytoplankton cell abundance (rDMS= 0.73 and rMeSH= 0.86), indicating an important role for this phytoplankton size class, and also its potential as a proxy for estimating DMS and MeSH emissions in chemistry-climate models.
Publisher: Informa UK Limited
Date: 11-11-2020
No related grants have been discovered for Maija Peltola.